54095-24-8Relevant articles and documents
Rodlike 4,6-diamino-1,3,5-triazine derivatives, effect of the core length on mesophase behavior and their application as LE-LCD device
Cao, Yu,Chang, Qing,Cheng, Xiaohong,Liu, Feng,Su, Fawu,Tan, Xiaoping
, (2021/11/16)
Three series of diaminotriazine derivatives with different core length have been synthesized, and the influence of the structural variation as well as the temperature on their mesophase behaviour were systematically investigated. With focus on the formation of CubI/Im3ˉm phase, multiple 2D/3D phases were discovered. Confirmed by polarized optical microscope, small/wide angle X-ray scattering, grazing incident small-angle X-ray scattering as well as molecular dynamics simulation, the results indicate that molecular curvature is critical to self-assembly structures. Moreover, the prerequisite for the formation of the CubI/Im3ˉm phase is intermediate molecular curvature on the surface of the micelle to allow the intercalation of the alkyl chains. Finally, the potentials for such compounds as light-emitting liquid crystal display (LE-LCD) device has been initially demonstrated.
Selective Mechanochemical Monoarylation of Unbiased Dibromoarenes by in Situ Crystallization
Seo, Tamae,Kubota, Koji,Ito, Hajime
supporting information, p. 9884 - 9889 (2020/05/19)
Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of liquid, unbiased dibromoarenes under mechanochemical conditions selectively afford the monoarylated products. The lower reactivity of the crystalline monoarylated products relative to the liquid starting materials should be attributed predominantly to the low diffusion efficiency of the former in the reaction mixture, which results in a selective monoarylation. The present study sheds light on a novel approach using in situ phase transitions in solids to design selective organic transformations that are difficult to achieve via conventional solution-based synthesis.
Effect of Thiophene Spacer Position in Carbazole-Based Dye-Sensitized Solar Cells on Photophysical, Electrochemical and Photovoltaic Properties
Samae, Ruslan,Surawatanawong, Panida,Eiamprasert, Utt,Pramjit, Songyos,Saengdee, Laksana,Tangboriboonrat, Pramuan,Kiatisevi, Supavadee
, p. 3536 - 3549 (2016/07/28)
The synthesis, photophysical and electrochemical properties, and photovoltaic performances in dye-sensitized solar cells (DSSCs) of five new metal-free organic sensitizers with a carbazole moiety as the electron donor are reported. The compounds contain a thiophene at various positions and a cyanoacrylic acid unit as the electron acceptor. The position of the thiophene moiety affected both the photophysical and electrochemical properties, leading to conversion efficiencies of 1.44 to 4.57 % under AM 1.5 solar conditions (100 mW cm–2). The best performance and longest electron lifetime were found when a thiophene was located on both donor and acceptor sites. The DSSC showed a short-circuit current (Jsc) of 8.59 mA/cm2, an open-circuit photovoltage (Voc) of 0.75 V, and a fill factor (FF) of 0.71. The position of the π-conjugated bridges not only affects the absorption spectra and the energy levels of the sensitizers, but also adjusts the electron lifetime.
